1. Regulations
  2. title 21
  3. chapter I-i7
  4. part 801
  5. subpart D
  6. § 801.122

View all text of Subpart D [§ 801.109 - § 801.128]

§ 801.122 - Medical devices for processing, repacking, or manufacturing.

A device intended for processing, repacking, or use in the manufacture of another drug or device shall be exempt from section 502(f)(1) of the act if its label bears the statement “Caution: For manufacturing, processing, or repacking”.

AUTHORITY: 21 U.S.C. 321, 331-334, 351, 352, 360d, 360i, 360j, 371, 374.

SOURCE: 41 FR 6896, Feb. 13, 1976, unless otherwise noted.

CITE AS: 21 CFR 801.122